Canonical Allele Identifier: CA803977606

Gene: MIR3936HG

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132364175A>T , CM000667.2:g.132364175A>T	GRCh38
NC_000005.9:g.131699867A>T , CM000667.1:g.131699867A>T	GRCh37
NC_000005.8:g.131727766A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.380+760T>A